Bipolar Medication Names & Facts Flashcards

1
Q

Drugs that may trigger mania

A
Amphetamines
Bromides- Sedative
Cocaine
Antidepressants
Isoniazid- anti TB drug
Procarbazine- Chemotherapy
Steroids
Stimulants
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2
Q

Dysregulation Theory

A

Not specific to bipolar but mood in general

Failure in some part of a homeostatic mechanism that regulates mood

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3
Q

Chaotic Attractor Theory

A

Biochemical defect leads to the dysregulation of neurotransmitter synthesis. Symptom presentation varies based on the physiological and environmental conditions at that time

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4
Q

Kindling Theory (Ballinger and Post)

A

Symptoms result of cumulative effects of subclinical biochemical changes in the limbic system

The progressive buildup causes neurons to become more excitable until symptoms appear

Progressive changes over time explain increased frequency and severity of episodes with aging

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5
Q

Catecholamine Theory

A

Noradrenergic abnormalities predominate and are measured by concentrations of norepinephrine and its major metabolite (MHPG)

Probably not the primary causative factor

Urinary levels of MHPG are lower in bipolar depressed and higher during mania

Levels also lower in bipolar depression than unipolar depression

In manin, CSF concentration of NE and MHPG are increased

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6
Q

Genetic and Familial Theories

A

Adoption, twin, and familial studies support that bipolar is heritable

Concordance rates for monozygotic twins 50-60% for bipolar

Chromosome 22 has been implicated in both bipolar disorder and schizophrenia

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7
Q

carbamazepine

A

(Tegretol)
Anticonvulsant (Note: 2nd generative anticonvulsants have significant side effects- limiting their use, also have birth defects) (& Mood Stabilizer)

Inhibits the release of glutamate (Equator is the extended release form)

Prescribed for acute mania, bipolar depression, bipolar maintenance

Must monitor serum levels (4-10 mcg/ml)

SE: Sedation dizziness, drowsiness, blurred vision, poor coordination, N/V, diarrhea, abdominal pain, decrease white blood cells, red, itching rash or hives, numerous drug reactions

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8
Q

lamotrigine

A

(Lamictal)
3rd generation anticonvulsant (& Mood stabilizer)

Effective for acute bipolar depression and RC bipolar II, as well as prevention of recurrent bipolar depressive episodes

Now the 1st line of treat for RC bipolar II

Less likely to cause a manic shift compared to other antidepressants

NOT used for acute mania

Rapidly absorbed

No monitoring of serum levels required

Can improve cognitive functioning

Adverse side effects increase with higher doses

SE: dizziness, tremors, somnolence, headache, nausea, rash ***Stevens-Johnsons syndrome risk (life threatening condition affecting the skin in which cell death cases the epidermis to separate from the dermis)– risk increases with concomitant use of divalproex

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9
Q

gabapentin

A

(Neurontin)
Anticonvulsant

Used to treat partial complex seizures, bipolar (not typically), anxiety, neuropathic pain, substance dependency, behavioral dyscontrol, and chronic headaches

Increases GABA levels but unclear how

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10
Q

pregabalin

A

(Lyrica)
Anticonvulsant

Derivative of gabapentin (but much more potent than gabapentin, 2-3 times as much)

Treats pains, seizures, fibromyalgia

Not specifically used for bipolar

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11
Q

topiramate

A

(Topamax)
Anticonvulsant

Used to prevent relapse to detrimental drinking patterns in people with alcoholism (common in patients with bipolar), also used to treat migraine headaches

Questionable effectiveness for bipolar

Weight LOSS as opposed to weight gain so can be used to offset the weight gain associated with other treatments

Excreted unchanged (meaning not metabolized by the liver) and reduced likelihood of drug interactions

Potential to increase plasma levels of other drugs excreted by kidneys, such as lithium

Increased incidence of kidney stones

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12
Q

zonisamide

A

(Zonegran)
Anticonvulsant

Mixed results in treatment of bipolar

High drop out rate due to side effects (worsening of mood, sedation, lack of effectiveness, more serious SE: decreased WBC, increased liver enzymes, drug interactions

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13
Q

oxcarbazepine

A

(Trileptal)
Anticonvulsant

Primarily used to treat seizures, but also treats bipolar, migraines, and nerve pain (although not FDA approved to treat these)

Trileptal is primarily exerted through its active metabolite (MHD)

Excreted by the kidneys

May cause the level of sodium in your blood to be dangerously low

Several drug interactions

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14
Q

valproate (aka valproic acid, sodium valproate, divalproex sodium)

A

(Depakote)
Anticonvulsant (& Mood Stabilizer)

FDA approved to treat epilepsy, bipolar, and migraines

Mostly metabolized in the liver. However, a small percentage absorbed by mitochondria

As with most anticonvulsants, mechanism unknown

Reduces the severity of mania, used to prevent long term recurrence of mania, in some cases has helped to lower depression associated with bipolar

Some SE: liver damage, suicidiality, anemia, pancreatitis, polycystic ovarian syndrome

interacts with anticoagulants, other anticonvulsants, drugs that depress the CNS (e.g., muscle relaxers)

Therapeutic window is small*

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15
Q

lithium

A

Lithobid
Mood stabilizer

For bipolar, first line= mood stabilizer (addresses mania), depression is addressed later with a different medication

Only 60-70% of those with bipolar disorder can be adequately controlled by lithium alone

Regulates mood, helps to decrease severity and frequency of mania

Lithium less effective in controlling RC mania- need for adjunct or alternative intervention for treatment resistant, noncompliance, or lithium side effects

Decreases risk of suicide

NOT protein bound

Absorption is rapid

No one really understand mechanism of action- but decreases excitatory transmission in neurons by lowering levels of dopamine and glutamate, and increases inhibitory transmissions by increasing levels of GABA and serotonin

1-3 weeks- therapeutic level, therapeutic window is small*

No antidote for lithium except for dialysis

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16
Q

bupropion

A

(Wellbutrin)
Antidepressant- NDRI (norepinephrine-dopamine reuptake inhibitor)

Inhibits dopamine and dopamine transporter (DAT) and norepinephrine and NE transporter (NET)

Absorbed in GI tract- overall absorption nearly 100%, but bioavailability of parent drug is less than 100% due to first pass metabolism

Does not bind to proteins at a significant level, but binds to DAT for up to 24 hours after treatment

Primarily metabolized in liver

half life= ~21 hours

Used for depression, smoking cessation, parkinson’s, bipolar

4 to 6 times more likely to lead to weight GAIN, sedation, or sexual side effects than SSRIs

Significant abuse potential (too much DAT occupancy= euphoria and reward)

17
Q

Difficult Cases

A

Typical antipsychotics:
Rispiradone - approved for mono therapy
Clozapine- approved for mono therapy

Olanzapine and fluoxetine si FDA approved for fixed dose combination of bipolar depression

18
Q

Key points to clients

A

Meds that treat current symptoms will also help prevent relapse – important to continue treatment after current episode is resolved

Since therapeutic and toxic dosage ranges (lithium) are so close, need to monitor blood level closely – never increase dose on your own

These meds are not addictive
Many SE may subside over time or be minimized by divided doses

These drugs cause birth defects – talk to provider immediately if find pregnant

Lifestyle Management is a critical ingredient

  • Regular bedtime and awakening time
  • Avoid sleep deprivation
  • Avoid shift work
  • Keep amount of bright sunlight exposure stable throughout the year
  • Avoid alcohol and illicit drug use
  • Avoid substances that interfere with sleep (caffeine, alcohol, minor tranquilizers, decongestants)
  • Avoid or limit travel across time zones